Covidien, LP

Frequent Recalls

6

Recalls

0

Units Recalled

0

Injuries

0

Deaths

Categories: Medical Device

2026-06-10 to 2026-08-19

Date	Source	Product	Brand	Severity	Units
2026-08-19	FDA Device	FDA Recall: V-Loc 90 Absorbable Wound Closure Device VLOC 90 0 VL 22 GS-21 VLOCM0336 VLOC 90 0 VL 22 G	Covidien, LP	Class II	N/A
2026-08-19	FDA Device	FDA Recall: V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING BOX06614V4 BOX BY P	Covidien, LP	Class II	N/A
2026-08-19	FDA Device	FDA Recall: Surgipro II S8698GX SURGIPRO II BL 5/0 18 P-13 S8698GX	Covidien, LP	Class II	N/A
2026-08-19	FDA Device	FDA Recall: Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623	Covidien, LP	Class II	N/A
2026-08-19	FDA Device	FDA Recall: Dermalon 88861757-31 DERMALON* 4-0 BLU 75CM C13 88861757-31 88861799-31 DERMALON* 4-0 BLU 7	Covidien, LP	Class II	N/A
2026-06-10	FDA Device	FDA Recall: Covidien EndoStitch" Polysorb Single Use Loading Unit; Product numbers: 170053 and 170071;	Covidien, LP	Class II	N/A

Covidien, LP Recalls | WatchRecall